A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987741



Internal ID12981490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19961836..20896789hg38UCSC Ensembl
Innerchr15:20167089..21102118hg19UCSC Ensembl
Innerchr15:18427103..19366762hg18UCSC Ensembl
Innerchr15:18427103..19366762hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38934954
hg19935030
hg18939660
hg17939660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751388
Supporting Variants
SamplesNA18971
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, POTEB, POTEB2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987741
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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